A concise total synthesis of (±)- and (-)-okilactomycin D.

Org Lett

Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, USA.

Published: February 2012

The spirotetronate okilactomycin D (7) has been efficiently synthesized by a route featuring a substrate-controlled, diastereoselective (8:1) intramolecular Diels-Alder (IMDA) reaction of 11. The assigned absolute configuration of (-)-7 was confirmed.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3272355PMC
http://dx.doi.org/10.1021/ol203355gDOI Listing

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